| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000346248 |
| Start |
124012399:124012399(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1429C>T |
| AA Mutation |
p.Arg477Cys(p.R477C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000346248 |
| Start |
124044704:124044704(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.762G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000346248 |
| Start |
124046053:124046053(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.160T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |